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Series GSE65730 Query DataSets for GSE65730
Status Public on Oct 30, 2015
Title Comprehensive role of Zfp217 in m6A methylation [ChIP-seq]
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Many transcriptional and epigenetic networks must be integrated to maintain self-renewal and pluripotency in embryonic stem cells (ESCs) and to enable induced pluripotent stem cell (iPSC) reprogramming. Here, we explore the role of Zfp217 as a key transcriptional factor in maintaining ES cell self-renewal by permorming genome-wide ChIP-Seq analyses.
 
Overall design Examination of Zfp217 binding profiling by high throughput sequencing in mouse stem cells
 
Contributor(s) Aguilo F, Zhang F, Zhang W, Walsh MJ
Citation(s) 26526723
Submission date Feb 06, 2015
Last update date May 15, 2019
Contact name Martin J. Walsh
E-mail(s) martin.walsh@mssm.edu
Organization name Mount Sinai School of Medicine
Department Structural and Chemical Biology
Street address One Gustave L. Levy Pl.
City New York
State/province NY
ZIP/Postal code 10029
Country USA
 
Platforms (1)
GPL9185 Illumina Genome Analyzer (Mus musculus)
Samples (2)
GSM1603861 Input_ChIP-seq
GSM1603862 Zfp217_ChIP-seq
This SubSeries is part of SuperSeries:
GSE65735 Comprehensive role of Zfp217 in m6A methylation
Relations
BioProject PRJNA274813
SRA SRP053314

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Supplementary file Size Download File type/resource
GSE65730_Znf217_ChIPseq_peaks.bed.gz 208.3 Kb (ftp)(http) BED
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Processed data are available on Series record

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